Triethylammonium acetate
Names
IUPAC name
Triethylammonium acetate
Other names
teaa, triethylamine/acetate buffer
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.023.632
  • InChI=1S/C6H15N.C2H4O2/c1-4-7(5-2)6-3;1-2(3)4/h4-6H2,1-3H3;1H3,(H,3,4) checkY
    Key: AVBGNFCMKJOFIN-UHFFFAOYSA-N checkY
  • InChI=1/C6H15N.C2H4O2/c1-4-7(5-2)6-3;1-2(3)4/h4-6H2,1-3H3;1H3,(H,3,4)
    Key: AVBGNFCMKJOFIN-UHFFFAOYAA
  • O=C([O-])C.CC[N+H](CC)CC
Properties
(CH3CH2)3NHOCOCH3
Molar mass 161.24 g/mol
Boiling point 164.5 °C (328.1 °F; 437.6 K)
Soluble
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
 Corrosive, harmful
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Triethylammonium acetate is a volatile salt, which is often used as an ion-pairing reagent in high-performance liquid chromatography separations of oligonucleotides.[1][2][3][4] Since unadjusted triethylammonium acetate salt solutions contain neither conjugate acid nor conjugate base, they are not buffers.

References

  1. ↑ "Triethylammonium Acetate, 1 M Solution - CAS 5204-74-0 - Calbiochem 625718". Sigma-Aldrich. Retrieved 2020-07-25.
  2. ↑ PubChem. "Triethylammonium acetate". pubchem.ncbi.nlm.nih.gov. Retrieved 2020-07-25.
  3. ↑ Berton, Paula; Kelley, Steven P.; Wang, Hui; Rogers, Robin D. (2018-11-01). "Elucidating the triethylammonium acetate system: Is it molecular or is it ionic?". Journal of Molecular Liquids. 269: 126–131. doi:10.1016/j.molliq.2018.08.006. ISSN 0167-7322. S2CID 106116704.
  4. ↑ "Solution Preparation". www.chem.uci.edu. Retrieved 2020-07-25.
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